Pages that link to "Q34021149"
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The following pages link to A high-density screen for linkage in multiple sclerosis (Q34021149):
Displaying 50 items.
- Early B-cell Factor gene association with multiple sclerosis in the Spanish population (Q21261385) (← links)
- Revealing the genetic basis of multiple sclerosis: are we there yet? (Q22252206) (← links)
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (Q24635370) (← links)
- Interrogating the major histocompatibility complex with high-throughput genomics (Q26822705) (← links)
- CCL genes in multiple sclerosis and systemic lupus erythematosus (Q28286163) (← links)
- Bayes factors in complex genetics (Q30497403) (← links)
- PRKCA and multiple sclerosis: association in two independent populations (Q33238942) (← links)
- Three allele combinations associated with multiple sclerosis (Q33251989) (← links)
- An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians (Q33252011) (← links)
- HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis (Q33291761) (← links)
- Increased prevalence of multiple sclerosis among COPD patients and their first-degree relatives: a population-based study (Q33324460) (← links)
- Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission (Q33325679) (← links)
- Mining for single nucleotide polymorphisms in pig genome sequence data (Q33397832) (← links)
- Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia (Q33490625) (← links)
- Large scale single nucleotide polymorphism discovery in unsequenced genomes using second generation high throughput sequencing technology: applied to turkey (Q33511017) (← links)
- Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis (Q33608541) (← links)
- A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01. (Q33622435) (← links)
- The genetic aspects of multiple sclerosis (Q33670899) (← links)
- Burden of genetic risk variants in multiple sclerosis families in the Netherlands (Q33693069) (← links)
- What role for genetics in the prediction of multiple sclerosis? (Q33695782) (← links)
- Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come (Q33772946) (← links)
- Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility (Q33790356) (← links)
- CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis (Q33832877) (← links)
- Whole-genome amplification enables accurate genotyping for microarray-based high-density single nucleotide polymorphism array (Q33855441) (← links)
- Environmental factors in early childhood are associated with multiple sclerosis: a case-control study (Q34041828) (← links)
- Meta-analysis of genome-wide linkage studies across autoimmune diseases (Q34325606) (← links)
- Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12. (Q34658050) (← links)
- Fine mapping and functional analysis of the multiple sclerosis risk gene CD6 (Q34701324) (← links)
- A genome-wide linkage screen in the Amish with Parkinson disease points to chromosome 6 (Q34801743) (← links)
- Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis (Q34993579) (← links)
- Genetics and pathogenesis of multiple sclerosis (Q35004746) (← links)
- Modification of Multiple Sclerosis Phenotypes by African Ancestry at HLA (Q35101408) (← links)
- Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans (Q35116360) (← links)
- Genome-wide homozygosity and multiple sclerosis in Orkney and Shetland Islanders (Q35679765) (← links)
- Role of the MHC2TA gene in autoimmune diseases. (Q35759959) (← links)
- Association between the ACCN1 gene and multiple sclerosis in Central East Sardinia (Q35794487) (← links)
- Genetic determinants of risk and progression in multiple sclerosis (Q35915818) (← links)
- An integrated approach to design novel therapeutic interventions for demyelinating disorders (Q36059972) (← links)
- HLA class I & II alleles in multiple sclerosis patients from Puerto Rico (Q36069652) (← links)
- Profile of differential promoter activity by nucleotide substitution at GWAS signals for multiple sclerosis (Q36154012) (← links)
- Myelin oligodendrocyte glycoprotein peptide-induced experimental allergic encephalomyelitis and T cell responses are unaffected by immunoproteasome deficiency (Q36329027) (← links)
- Progress in multiple sclerosis genetics (Q36382352) (← links)
- Using high-throughput SNP technologies to study cancer (Q36426758) (← links)
- Finding disease candidate genes by liquid association (Q36465598) (← links)
- Application of oligonucleotide arrays to high-content genetic analysis (Q36481133) (← links)
- No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis (Q36780814) (← links)
- Genetics in multiple sclerosis: past and future perspectives. (Q36785946) (← links)
- Class II HLA interactions modulate genetic risk for multiple sclerosis (Q36920509) (← links)
- Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations (Q36930892) (← links)
- Recent advances in genetic analysis of multiple sclerosis: genetic associations and therapeutic implications (Q36941912) (← links)